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HGB/WIC LYSE - India CDSCO Medical Device Registration

HGB/WIC LYSE is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000419_e28636bcd5c586b570dc58338d4719f6_0f528bf53743c087b09b97a532e376d0. This device is marketed under the brand name DILUENT/SHEATH. The license holder is Abbott Healthcare Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is CDSCO.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class B
HGB/WIC LYSE
UID: IMP/IVD/2019/000419_e28636bcd5c586b570dc58338d4719f6_0f528bf53743c087b09b97a532e376d0

Brand Name

DILUENT/SHEATH

Device Class

Class B

Approving Authority

CDSCO

Product Information

Lyse the RBC and minimize the resultant stroma. Strip the white cell cytoplasm. Convert HGB to modified hemiglobincyanide complex

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